Branch No: 67407-7241
850 Chelmsford Street
Suite 5
Lowell, MA 01851
Phone: (978) 674-5455

Available Positions

9 positions available.

Production Planner

Wilmington MA

Base Pay: Depends on Experience

Local, in person interviews Perm Assist in setting the site capacity plan to align with the sales from the integrated business plan, while meeting...

Local, in person interviews

Perm

Assist in setting the site capacity plan to align with the sales from the integrated business plan, while meeting business objectives of safety, quality, on-time delivery, competitive customer lead times, profitability and inventory. Coordinate and expedite the flow of work and materials within or between departments according to the plan while achieving customer requirements. Work closely with functional teams to determine progress of work, completion dates, and production problems with parts. Identify and resolve job costing issues and other accounting problems associated with work in process problems. Need Bachelor’s degree and 5 to 8 years of relevant experience.

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Process Safety Engineer

Nashua NH

Base Pay: Depends on Experience

Local Candidates only Face to Face interviews No relocation   Responsibilities • Ability to draft project budgets, timeline and outline c...

Local Candidates only

Face to Face interviews

No relocation

 

Responsibilities • Ability to draft project budgets, timeline and outline critical paths to complete. • Working with Development chemists, Supervisors and outside Engineering vendors to design/size process equipment. • Coordinating with Development Chemists to develop, configure and optimize new processes – through inception through to start up and certification. • Coordinating with Facilities, Manufacturing and Maintenance to establish equipment installation plans, mechanical integrity testing and start-up procedures, as necessary. • Develop methods and innovative solutions to improve production rates. • Manage cost and time constraints. • Performing material and energy balances as part of Chemical Process Improvement program. • Generating process schematics, PFDs/P&ID, and LO-TO diagrams. • Provide SOPs (operating instruction) for various processes and equipment. • Troubleshooting with operators and supervisors as needed. • Investigate current processes and conditions, and offer process, safety and quality improvements. • Investigation and assessment of process parameters; collect and interpret data including temperatures, pressures, flow rates, composition, etc. • Performing risk assessments in a team-based setting. • Coordinating with Sustainability group and Quality/Environmental engineer as needed to assist in various environmental obligations.

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Automation/Control Engineer

Westborough MA

Base Pay: DOE

In person interviews Local Candidates Perm opportunity Primary Purpose:   Automation Engineer with a minimum of 8+ years of experience with Ro...

In person interviews

Local Candidates

Perm opportunity

Primary Purpose:  

Automation Engineer with a minimum of 8+ years of experience with Rockwell PLC's to provide operational support in a bio-pharmaceutical environment.  Candidate will be responsible for fielding support requests from manufacturing and facilities personnel and provide hardware and software troubleshooting assistance.  This individual would also propose potential solutions to issues identified with equipment and systems.  Documentation and execution of changes would follow the customer’s change control process.

Essential Responsibilities:

  • Assess and record requests for assistance.  Gather necessary information and identify personnel required for assistance.
  • Understand customer standard operating procedures
  • Analyze a running system using PLC code to determine the root cause of an issue
  • Communicate information back to responsible parties
  • Read and understand system drawings and design documents
  • Document findings using customer procedures
  • Develop solutions to known issues and document in a detailed change description
  • Create a technical evaluation and test plan using customer supplied templates
  • Update system drawings and design documents to reflect modifications
  • Execute a change control and associated test plan

Requirements:

  • Bachelor’s Degree Required, Candidate should have BS ChemE, MechE or BioE – Or equivalent experience and education will be considered
  • Minimum of 8 years of experience with Rockwell
  • Experience working in the Bio-pharmaceutical industry (cGMP manufacturing, pilot plants, and laboratories)  a plus
  • Practical experience with control systems (PLC, DCS, Loop controllers)
  • Strong understanding of the latest ASME Bioprocess Equipment standards 

Experience working in the Bio-pharmaceutical industry (cGMP manufacturing, pilot plants, and laboratories) a plus Practical experience with control systems (PLC, DCS, Loop controllers) Strong understanding of the latest ASME Bioprocess Equipment standards

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Automation/Control Engineer Siemens S7

Albany NY

Base Pay: DOE

Local Candidates In person interview Perm Opportunity Primary Purpose:   Automation Engineer with 3+ years of experience to provide operationa...

Local Candidates

In person interview

Perm Opportunity

Primary Purpose:  

Automation Engineer with 3+ years of experience to provide operational support.  Candidate will be responsible for fielding support requests from manufacturing and facilities personnel and provide hardware and software troubleshooting assistance.  This individual would also propose potential solutions to issues identified with equipment and systems.  Documentation and execution of changes would follow the customer’s change control process.

Essential Responsibilities:

Assess and record requests for assistance. 

Gather necessary information and identify personnel required for assistance. 
Understand customer standard operating procedures. 
Analyze a running system using PLC code to determine the root cause of an issue. 
Communicate information back to responsible parties. 
Read and understand system drawings and design documents. 
Document findings using customer procedures. 
Develop solutions to known issues and document in a detailed change description. 
Create a technical evaluation and test plan using customer supplied templates. 
Update system drawings and design documents to reflect modifications. 
Execute a change control and associated test plan.


Knowledge, Abilities, Skills: 
Read and understand piping and instrumentation diagrams (P&ID). 
Read and understand control system electrical drawings. 
Proficient with Allen Bradley PLC systems.  Ability to read and understand PLC code. 
Read and understand system life cycle documents such as the User Requirements Specification (URS), Functional Specification (FS), and Software Design Specification (SDS). 
Familiarity with equipment used in a Biotech facility such as Bioreactors, Mixing Tanks, Filtration Systems, Clean Utilities, and CIP is a plus. 
Knowledge of Good Automated Manufacturing Practice (GaMP) is a plus. 
Knowledge of Good Documentation Practice (GDP) is a plus. 
Proficiency with Siemens S7 PLC systems and FactoryTalk View ME/SE is a plus.

Requirements:

A minimum of an Associate's Degree in Engineering 
3+ years of industrial controls experience 
Proficient with Allen Bradley PLC systems

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Validation Engineer

Westborough MA

Base Pay: DOE

In Person interviews Perm Opportunity Local Candidates Validation Engineer with 2+ years of experience to provide validation and documentation supp...

In Person interviews

Perm Opportunity

Local Candidates

Validation Engineer with 2+ years of experience to provide validation and documentation support. Incumbent will be responsible for review and update of system life cycle documents (URS, FS, HDS, SDS), creation of traceability matrices, and the creation of test plans.

This individual will also be responsible for the execution of test procedures and review of executed test plans.

Essential Responsibilities: Assess and record requests for assistance. Gather necessary information and identify personnel required for assistance Understand customer standard operating procedures Communicate information back to responsible parties Update system documents based on new product releases Assist in the development of engineering change requests Perform an impact assessment on documents based on system modifications K

nowledge, Abilities, Skills: Read and understand system life cycle documents such as the User Requirements Specification (URS), Functional Specification (FS), and Software Design Specification (SDS) Familiarity with equipment used in a Biotech facility such as Bioreactors, Mixing Tanks, Filtration Systems, Clean Utilities, and CIP is a plus Knowledge of Good Automated Manufacturing Practice (GaMP) Knowledge of Good Documentation Practice (GDP) Familiarity with automation equipment such as Programmable Logic Controllers (PLCs) is a plus

Requirements: Bachelor’s Degree in Engineering 2+ years of validation experience Knowledge of Good Automated Manufacturing Practice (GaMP)

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Automation/Control Engineer - Wonderware

Westborough MA

Base Pay: DOE

Local, In person interviews. Start ASAP   Primary Purpose: Automation Engineer with ArchestrA System Platform experience, will be pr...

Local, In person interviews.

Start ASAP

 

Primary Purpose:

Automation Engineer with ArchestrA System Platform experience, will be providing support in a bio-pharmaceutical environment.

Candidate will be responsible for requests from manufacturing and facilities personnel and provide hardware and software troubleshooting assistance.

This individual would also propose potential solutions to issues identified with equipment and systems.

Documentation and execution of changes would follow the customer’s change control process.

Essential Responsibilities: • Assess and record requests for assistance. Gather necessary information and identify personnel required for assistance. • Understand customer standard operating procedures • Communicate information back to responsible parties • Read and understand system drawings and design documents • Document findings using customer procedures • Develop solutions to known issues and document in a detailed change description • Create a technical evaluation and test plan using customer supplied templates • Update system drawings and design documents to reflect modifications • Execute a change control and associated test plan

Requirements: • Bachelor’s Degree Required, Candidate should have BS ChemE, MechE or BioE – Or equivalent experience • Minimum of 2 years of experience with Wonderware Archestra • Experience working in the Bio-pharmaceutical industry (cGMP manufacturing, pilot plants, and laboratories) a plus • Knowledge of control systems (PLC, DCS, Loop controllers) • Strong understanding of the latest ASME Bioprocess Equipment standards

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Buyer

Wilmington MA

Base Pay: DOE

Local Candidates only In person interviews Temp/Temp to perm Seeking an experienced buyer to work for a medical device contract manufacturer. Perso...

Local Candidates only

In person interviews

Temp/Temp to perm

Seeking an experienced buyer to work for a medical device contract manufacturer. Person would be responsible for obtaining quotes, negotiating and purchasing various raw materials, consumables and services for the company. Duties to include maintaining ERP stocking levels and working with Planners and Production personnel to assure the timely ordering and delivery of materials. Must have minimum of one year of experience working with ERP system in an industrial manufacturing company. Experience in purchasing steel and/or titanium preferred. Good excel skills required.

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Manufacturing Engineer

Woburn MA

Base Pay: 60-65K

Woburn MA  Bachelor’s Degree in Engineering    3 years of experience working in a manufacturing environment.  Knowledge o...

Woburn MA 

Bachelor’s Degree in Engineering 

 

3 years of experience working in a manufacturing environment. 

Knowledge of manufacturing methods with lathes, mills and advanced machine centers a plus. 

Generate operations sheets from viable operational sequences for future, as well as, existing production needs. 

This position may require design of tools, fixtures and gages to support manufacturing spinal and extremity implants. 

Candidate should have strong modeling and drafting skill and working knowledge of geometric  and tolerance. E

 Solidworks and Unigraphics NX

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Quality Engineer

Wilmington MA

Base Pay: DOE

Bachelor’s degree in Engineering (mechanical preferred) and minimum 5 years’ experience working in the medical or aerospace manufacturi...

Bachelor’s degree in Engineering (mechanical preferred) and minimum 5 years’ experience working in the medical or aerospace manufacturing industries. Ensure compliance to ISO9001, ISO13485, AS9100 and FDA CFR820. Responsible for the development of part specific quality plans based on customer requirements in a manufacturing environment. Experience in geometric tolerances, ability to read blueprints and interpret to ANSI specifications. Must have a good understanding and ability to develop and document Risk Assessment, FMEA and Process Control Plans, CAPA activities. Candidate must have excellent communication, organizational and computer skills. CQE, CQA, or Green Belt a plus.

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Staff Bios

Paul Bordonaro General Manager - Metro Division
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Timothy Hovey Executive Search Manager
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  • Started with the company January 2018
  • Has 18 years of staffing industry experience
Amanda Scappaticci Executive Recruiter
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